MAUDE Adverse Event Report: IMPLANT DIRECT SYBRON MANUFACTURING LLC INTERACTIVE GPS ABUTMENT NARROW; DENTAL IMPLANT

Catalog Number 6530-95N

Device Problem Osseointegration Problem (3003)

Patient Problems Failure of Implant (1924); No Information (3190)

Event Type  malfunction  

Manufacturer Narrative

Per the complaint, lot information is unknown.If additional information becomes available a follow-up report will be submitted.

Event Description

Per complaint (b)(4), during clinical procedure, components could not be separated.

• Brand Name: INTERACTIVE GPS ABUTMENT NARROW
• Type of Device: DENTAL IMPLANT
• Manufacturer (Section D): IMPLANT DIRECT SYBRON MANUFACTURING LLC; 3050 east hillcrest drive; thousand oaks CA 91362
• Manufacturer Contact: adrienne stott ; 3050 east hillcrest drive; thousand oaks, CA 91362 ; 8184443300
• MDR Report Key: 9465219
• MDR Text Key: 170737476
• Report Number: 3001617766-2019-05744
• Device Sequence Number: 1
• Product Code: NHA
• UDI-Device Identifier: 10841307109754
• UDI-Public: 10841307109754
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: K143011
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: health professional,user faci
• Reporter Occupation: Dentist
• Remedial Action: Inspection
• Type of Report: Initial
• Report Date: 12/13/2019

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 12/13/2019
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Catalogue Number: 6530-95N
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: Yes
• Date Manufacturer Received: 11/19/2019
• Was Device Evaluated by Manufacturer?: No
• Is the Device Single Use?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Initial
• Patient Sequence Number: 1
• Patient Outcome(s): Required Intervention